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Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report
RATIONALE: Programmed cell death-1 protein (PD-1) antibody is an immune-checkpoint inhibitor that triggers anti-tumor response by enhancing immune response. Although PD-1 antibody has been reported effective in some malignant tumor, it can also induce significant immune-related adverse events (irAEs...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250450/ https://www.ncbi.nlm.nih.gov/pubmed/30407284 http://dx.doi.org/10.1097/MD.0000000000012907 |
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author | Li, Sicheng Zhang, Yi Sun, Zhichun Hu, Ji Fang, Chen |
author_facet | Li, Sicheng Zhang, Yi Sun, Zhichun Hu, Ji Fang, Chen |
author_sort | Li, Sicheng |
collection | PubMed |
description | RATIONALE: Programmed cell death-1 protein (PD-1) antibody is an immune-checkpoint inhibitor that triggers anti-tumor response by enhancing immune response. Although PD-1 antibody has been reported effective in some malignant tumor, it can also induce significant immune-related adverse events (irAEs) such as autoimmune diabetes. PATIENT CONCERNS: A 67-year-old male patient with non-small cell lung cancer (NSCLS) presented with polydipsia, polyuria, weakness, and weight loss after use of anti-programmed cell death-1 antibody therapy. Hyperglycemia, high serum ketone, low bicarbonate and high anion gap were compatible with the criteria of diabetic ketoacidosis (DKA). DIAGNOSES: Autoimmune diabetes and diabetic ketoacidosis (DKA). The presence of low serum titers of c-peptide, high blood glucose together with diabetic ketoacidosis (DKA) that occurs shortly after the use of pembrolizumab strongly supported the diagnosis of anti-PD-1 induced autoimmune diabetes. INTERVENTIONS: The patient stopped using pembrolizumab while continuous subcutaneous insulin infusion (CSII) was started at the same time. The insulin infusion was switched to multiple daily injection (MDI) after he was discharged from hospital. OUTCOMES: The patient is now a well-controlled insulin-dependent patient with palliative care of NSCLS. LESSONS: Autoimmune diabetes induced by anti-programmed cell death-1 (PD-1)/programmed cell death 1 ligand 1 (PD-L1) therapy is a rare, but life threatening immune-related side effect. Physicians should closely monitor diabetes-related indexes of patients who have been undergoing the treatment of anti-PD-1/PD-L1 therapy. |
format | Online Article Text |
id | pubmed-6250450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-62504502018-12-10 Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report Li, Sicheng Zhang, Yi Sun, Zhichun Hu, Ji Fang, Chen Medicine (Baltimore) Research Article RATIONALE: Programmed cell death-1 protein (PD-1) antibody is an immune-checkpoint inhibitor that triggers anti-tumor response by enhancing immune response. Although PD-1 antibody has been reported effective in some malignant tumor, it can also induce significant immune-related adverse events (irAEs) such as autoimmune diabetes. PATIENT CONCERNS: A 67-year-old male patient with non-small cell lung cancer (NSCLS) presented with polydipsia, polyuria, weakness, and weight loss after use of anti-programmed cell death-1 antibody therapy. Hyperglycemia, high serum ketone, low bicarbonate and high anion gap were compatible with the criteria of diabetic ketoacidosis (DKA). DIAGNOSES: Autoimmune diabetes and diabetic ketoacidosis (DKA). The presence of low serum titers of c-peptide, high blood glucose together with diabetic ketoacidosis (DKA) that occurs shortly after the use of pembrolizumab strongly supported the diagnosis of anti-PD-1 induced autoimmune diabetes. INTERVENTIONS: The patient stopped using pembrolizumab while continuous subcutaneous insulin infusion (CSII) was started at the same time. The insulin infusion was switched to multiple daily injection (MDI) after he was discharged from hospital. OUTCOMES: The patient is now a well-controlled insulin-dependent patient with palliative care of NSCLS. LESSONS: Autoimmune diabetes induced by anti-programmed cell death-1 (PD-1)/programmed cell death 1 ligand 1 (PD-L1) therapy is a rare, but life threatening immune-related side effect. Physicians should closely monitor diabetes-related indexes of patients who have been undergoing the treatment of anti-PD-1/PD-L1 therapy. Wolters Kluwer Health 2018-11-09 /pmc/articles/PMC6250450/ /pubmed/30407284 http://dx.doi.org/10.1097/MD.0000000000012907 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Research Article Li, Sicheng Zhang, Yi Sun, Zhichun Hu, Ji Fang, Chen Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title | Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title_full | Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title_fullStr | Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title_full_unstemmed | Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title_short | Anti-PD-1 pembrolizumab induced autoimmune diabetes in Chinese patient: A case report |
title_sort | anti-pd-1 pembrolizumab induced autoimmune diabetes in chinese patient: a case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250450/ https://www.ncbi.nlm.nih.gov/pubmed/30407284 http://dx.doi.org/10.1097/MD.0000000000012907 |
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